A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695521



Internal ID15085487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14652475..14655169hg38UCSC Ensembl
Innerchr8:14509984..14512678hg19UCSC Ensembl
Innerchr8:14554355..14557049hg18UCSC Ensembl
Innerchr8:14554355..14557049hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382695
hg192695
hg182695
hg172695
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695521
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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